MEXILETINE HYDROCHLORIDE (MEXILETINE HYDROCHLORIDE) — FDA Approval ANDA074450 (ANI PHARMS)
MEXILETINE HYDROCHLORIDE (MEXILETINE HYDROCHLORIDE) — FDA Approval ANDA074450 (ANI PHARMS) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: MEXILETINE HYDROCHLORIDE; Active ingredients: MEXILETINE HYDROCHLORIDE; Application number: ANDA074450.
| Brand name | MEXILETINE HYDROCHLORIDE |
|---|---|
| Active ingredients | MEXILETINE HYDROCHLORIDE |
| Application number | ANDA074450 |
| Sponsor | ANI PHARMS |
| Dosage form | CAPSULE |
| Route | ORAL |
| Marketing status | Prescription |
| Products in application | 3 |
| First approval date | 19960516 |
| Source | openFDA Drugs@FDA |
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